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α-(4-chloro-phenylsulfanyl)-isobutyric acid ethyl ester | 2004-19-5

中文名称
——
中文别名
——
英文名称
α-(4-chloro-phenylsulfanyl)-isobutyric acid ethyl ester
英文别名
α-(4-Chlor-phenylmercapto)-isobuttersaeure-aethylester;2-(4-chloro-phenylsulfanyl)-2-methyl-propionic acid ethyl ester;-isobuttersaeure-aethylester;Ethyl 2-(4-chlorophenyl)sulfanyl-2-methylpropanoate
α-(4-chloro-phenylsulfanyl)-isobutyric acid ethyl ester化学式
CAS
2004-19-5
化学式
C12H15ClO2S
mdl
——
分子量
258.769
InChiKey
WKVQILUSBBMPJB-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    46 °C(Solv: ligroine (8032-32-4))
  • 沸点:
    328.3±27.0 °C(Predicted)
  • 密度:
    1.18±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.9
  • 重原子数:
    16
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    51.6
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • Compounds Which Modulate The CB2 Receptor
    申请人:BERRY Angela
    公开号:US20080039464A1
    公开(公告)日:2008-02-14
    Compound of formula (I) are disclosed. Compounds according to the invention bind to and are agonists, antagonists or inverse agonists of the CB2 receptor, and are useful for treating inflammation. Those compounds which are agonists are additionally useful for treating pain.
    本发明揭示了化合物的公式(I)。根据本发明的化合物与CB2受体结合,并且是激动剂、拮抗剂或逆激动剂,适用于治疗炎症。那些是激动剂的化合物还可用于治疗疼痛。
  • Compounds Which Modulate the CB2 Receptor
    申请人:BERRY Angela
    公开号:US20110071127A1
    公开(公告)日:2011-03-24
    Compounds of formula (I) are disclosed. Compounds according to the invention bind to and are agonists, antagonists or inverse agonists of the CB2 receptor, and are useful for treating inflammation. Those compounds which are agonists are additionally useful for treating pain.
    公式(I)的化合物被披露。本发明的化合物与CB2受体结合,并且是激动剂、拮抗剂或反向激动剂,可用于治疗炎症。那些是激动剂的化合物还可用于治疗疼痛。
  • Compounds Which Selectively Modulate The CB2 Receptor
    申请人:BARTOLOZZI Alessandra
    公开号:US20100081644A1
    公开(公告)日:2010-04-01
    Compounds of formula (I) are disclosed. Compounds according to the invention bind to and are agonists, antagonists or inverse agonists of the CB2 receptor, and are useful for treating inflammation. Those compounds which are agonists are additionally useful for treating pain.
    公开了化学式(I)的化合物。本发明的化合物与CB2受体结合并且是激动剂、拮抗剂或反向激动剂,可用于治疗炎症。那些是激动剂的化合物还可用于治疗疼痛。
  • Therapeutic Uses of Compounds Which Selectively Modulate The CB2 Receptor
    申请人:BARTOLOZZI Alessandra
    公开号:US20110312932A1
    公开(公告)日:2011-12-22
    Compounds of formula (I) are disclosed. Compounds according to the invention bind to and are agonists, antagonists or inverse agonists of the CB2 receptor, and are useful for treating inflammation. Those compounds which are agonists are additionally useful for treating pain.
    本发明揭示了式(I)的化合物。该发明的化合物与CB2受体结合并且是激动剂、拮抗剂或反向激动剂,可用于治疗炎症。那些是激动剂的化合物还可用于治疗疼痛。
  • COMPOUNDS WHICH MODULATE THE CB2 RECEPTOR
    申请人:Bartolozzi Alessandra
    公开号:US20120316173A1
    公开(公告)日:2012-12-13
    Compounds of formula (I) are disclosed. Compounds according to the invention bind to and are agonists, antagonists or inverse agonists of the CB2 receptor, and are useful for treating inflammation. Those compounds which are agonists are additionally useful for treating pain.
    公式(I)的化合物已被揭示。本发明的化合物与CB2受体结合,并且是激动剂、拮抗剂或反向激动剂,可用于治疗炎症。那些是激动剂的化合物还可用于治疗疼痛。
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